Evidence map›Paper›PMID 40130080›Full record

ArticleBioactive materials2025

A self-accelerating 'copper bomb' strategy activated innate and adaptive immune response against triple-negative breast cancer.

Xinzhi Xu, Hang Zhou, Ruixia Hong, Jiaqi Gong, Yujie Wan, Qihuan Fu, Kaifeng Huang, Ying Li, Na Wang, Peng Zhao and 2 more

Erratum issuedAbstract read
In one paragraph

Article in Bioactive materials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Xinzhi XuDepartment of Ultrasound, Chongqing University Cancer Hospital, Chongqing 400030, China.
Hang ZhouDepartment of Ultrasound, Chongqing University Cancer Hospital, Chongqing 400030, China.
Ruixia HongDepartment of Ultrasound, Chongqing University Cancer Hospital, Chongqing 400030, China.
Jiaqi GongDepartment of Ultrasound, Chongqing University Cancer Hospital, Chongqing 400030, China.
Yujie WanDepartment of Ultrasound, Chongqing University Cancer Hospital, Chongqing 400030, China.
Qihuan FuDepartment of Ultrasound, Chongqing University Cancer Hospital, Chongqing 400030, China.
Kaifeng HuangDepartment of Ultrasound, Chongqing University Cancer Hospital, Chongqing 400030, China.
Ying LiDepartment of Ultrasound, Chongqing University Cancer Hospital, Chongqing 400030, China.
Na WangDepartment of Ultrasound, Chongqing University Cancer Hospital, Chongqing 400030, China.
Peng ZhaoKey Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Chongqing University, Chongqing 400044, China.
Kaiyong CaiKey Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Chongqing University, Chongqing 400044, China.
Fang LiDepartment of Ultrasound, Chongqing University Cancer Hospital, Chongqing 400030, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) presents therapeutic challenges due to its aggressive, drug-resistance, and low immunological reactivity. Cuproptosis, an emerging therapeutic modality, is a promising strategic intervention for treating TNBC. Nonetheless, the effectiveness of cuproptosis is compromised by tumor adaptations, including the Warburg effect, increased intracellular glutathione (GSH), and copper efflux, thus breaking the barrier of cuproptosis is the basis for developing cuproptosis-based clinical therapies. Herein, a self-accelerating strategy utilizing a pH-responsive copper framework encapsulating glucose oxidase (GOx), modified with polyethylene glycol (PEG) and tumor-penetrating peptide (tLyp1) has been developed. Upon reaching the acidic tumor microenvironment, the released GOx increases intracellular acidity and hydrogen peroxide (H

Indexed as

CuproptosisImmune responsemtDNA-cGAS-STING pathwayProteotoxic stressTriple-negative breast cancer

Identifiers

PMID40130080
PMCPMC11931225

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.